Oxidant-induced injury to the lung causes extensive damage to lung epithelial cells. Impaired protection and repair of the lung epithelium can result in death. The serine-threonine kinase Akt has been implicated in inhibiting cell death induced by different stimuli including growth factor withdrawal, cell cycle discordance, DNA damage, and loss of cell adhesion in different cell types. However, the in vivo relevance of this prosurvival pathway has not been explored. Here we show that a constitutively active form of Akt introduced intratracheally into the lungs of mice by adenovirus gene transfer techniques protects mice from hyperoxic pulmonary damage and delays death of mice. This is the first demonstration of the in vivo protective function of Akt in the context of oxidant-induced lung injury.
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19 February 2001
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February 20 2001
Activated Akt Protects the Lung from Oxidant-Induced Injury and Delays Death of Mice
Yunbiao Lu,
Yunbiao Lu
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
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Lisa Parkyn,
Lisa Parkyn
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
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Leo E. Otterbein,
Leo E. Otterbein
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
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Yasuko Kureishi,
Yasuko Kureishi
bDivision of Cardiovascular Research, St. Elizabeth's Medical Center and Program in Cell, Molecular and Developmental Biology, Sackler School of Biomedical Studies, Tufts University School of Medicine, Boston, Massachusetts 02135
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Kenneth Walsh,
Kenneth Walsh
bDivision of Cardiovascular Research, St. Elizabeth's Medical Center and Program in Cell, Molecular and Developmental Biology, Sackler School of Biomedical Studies, Tufts University School of Medicine, Boston, Massachusetts 02135
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Anuradha Ray,
Anuradha Ray
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
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Prabir Ray
Prabir Ray
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
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Yunbiao Lu
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
Lisa Parkyn
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
Leo E. Otterbein
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
Yasuko Kureishi
bDivision of Cardiovascular Research, St. Elizabeth's Medical Center and Program in Cell, Molecular and Developmental Biology, Sackler School of Biomedical Studies, Tufts University School of Medicine, Boston, Massachusetts 02135
Kenneth Walsh
bDivision of Cardiovascular Research, St. Elizabeth's Medical Center and Program in Cell, Molecular and Developmental Biology, Sackler School of Biomedical Studies, Tufts University School of Medicine, Boston, Massachusetts 02135
Anuradha Ray
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
Prabir Ray
aDepartment of Internal Medicine, Pulmonary and Critical Care Section, Yale University School of Medicine, New Haven, Connecticut 06520
Received:
November 22 2000
Revision Requested:
December 21 2000
Accepted:
January 03 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 193 (4): 545–550.
Article history
Received:
November 22 2000
Revision Requested:
December 21 2000
Accepted:
January 03 2001
Citation
Yunbiao Lu, Lisa Parkyn, Leo E. Otterbein, Yasuko Kureishi, Kenneth Walsh, Anuradha Ray, Prabir Ray; Activated Akt Protects the Lung from Oxidant-Induced Injury and Delays Death of Mice. J Exp Med 19 February 2001; 193 (4): 545–550. doi: https://doi.org/10.1084/jem.193.4.545
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